Canonical Allele Identifier: CA1200472526
Gene: LMNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156136223G= , CM000663.2:g.156136223G= GRCh38
NC_000001.10:g.156106014G= , CM000663.1:g.156106014G= GRCh37
NC_000001.9:g.154372638G= NCBI36
NG_008692.2:g.58651G= , LRG_254:g.58651G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504687.7:c.609G= ENSP00000426535.3:p.Leu203=
ENST00000498722.3:n.399G=
ENST00000682650.1:c.1167G= ENSP00000506904.1:p.Leu389=
ENST00000683032.1:c.1167G= ENSP00000506771.1:p.Leu389=
ENST00000684195.1:c.1167G= ENSP00000508220.1:p.Leu389=
ENST00000361308.9:c.1167G= ENSP00000355292.6:p.Leu389=
ENST00000368300.9:c.1167G= MANE Select ENSP00000357283.4:p.Leu389=
ENST00000496738.6:n.1542G=
ENST00000674518.1:c.*517G= ENSP00000502261.1:n.*517G=
ENST00000674600.1:c.*966G= ENSP00000501666.1:n.*966G=
ENST00000674720.1:c.1167G= ENSP00000502798.1:p.Leu389=
ENST00000675431.1:n.860G=
ENST00000675455.1:c.*967G= ENSP00000501795.1:n.*967G=
ENST00000675667.1:c.1167G= ENSP00000501803.1:p.Leu389=
ENST00000675874.1:c.*638G= ENSP00000501851.1:n.*638G=
ENST00000675881.1:c.*178G= ENSP00000501670.1:n.*178G=
ENST00000675939.1:c.1167G= ENSP00000502256.1:p.Leu389=
ENST00000675989.1:n.1542G=
ENST00000676208.1:c.*270G= ENSP00000502468.1:n.*270G=
ENST00000676283.1:n.1542G=
ENST00000676385.2:c.1167G= ENSP00000502091.1:p.Leu389=
ENST00000676434.1:c.*178G= ENSP00000501648.1:n.*178G=
ENST00000677389.1:c.1167G= MANE Plus Clinical ENSP00000503633.1:p.Leu389=
ENST00000347559.6:c.1167G= ENSP00000292304.3:p.Leu389=
ENST00000361308.8:c.1167G= ENSP00000355292.5:p.Leu389=
ENST00000368297.5:c.924G= ENSP00000357280.1:p.Leu308=
ENST00000368298.2:n.431G=
ENST00000368299.7:c.1167G= ENSP00000357282.3:p.Leu389=
ENST00000368300.8:c.1167G= ENSP00000357283.4:p.Leu389=
ENST00000368301.6:c.1167G= ENSP00000357284.2:p.Leu389=
ENST00000448611.6:c.831G= ENSP00000395597.2:p.Leu277=
ENST00000473598.6:c.870G= ENSP00000421821.1:p.Leu290=
ENST00000496738.5:n.552G=
ENST00000498722.2:n.399G=
ENST00000508500.1:c.45G= ENSP00000424977.1:p.Leu15=
NM_001257374.2:c.831G= NP_001244303.1:p.Leu277=
NM_001282624.1:c.924G= NP_001269553.1:p.Leu308=
NM_001282625.1:c.1167G= NP_001269554.1:p.Leu389=
NM_001282626.1:c.1167G= NP_001269555.1:p.Leu389=
NM_005572.3:c.1167G= , LRG_254t1:c.1167G= NP_005563.1:p.Leu389=
NM_170707.3:c.1167G= NP_733821.1:p.Leu389=
NM_170708.3:c.1167G= NP_733822.1:p.Leu389=
XM_011509533.1:c.831G= XP_011507835.1:p.Leu277=
XM_011509534.1:c.543G= XP_011507836.1:p.Leu181=
XR_921781.1:n.1456G=
XM_011509534.2:c.543G= XP_011507836.1:p.Leu181=
XR_921781.2:n.1454G=
NM_170707.4:c.1167G= MANE Select NP_733821.1:p.Leu389=
NM_001257374.3:c.831G= NP_001244303.1:p.Leu277=
NM_001282626.2:c.1167G= NP_001269555.1:p.Leu389=
NM_001282624.2:c.924G= NP_001269553.1:p.Leu308=
NM_001282625.2:c.1167G= NP_001269554.1:p.Leu389=
NM_005572.4:c.1167G= MANE Plus Clinical NP_005563.1:p.Leu389=
NM_170708.4:c.1167G= NP_733822.1:p.Leu389=